Skip to the page

Data / Medical devices / China / Micowey Medical Equipment Guangxi Co., Ltd

Micowey Medical Equipment Guangxi Co., Ltd: FDA-registered device maker in Wuzhou Guangxi, China, 1 510(k) clearance

Micowey Medical Equipment Guangxi Co., Ltd is registered with the FDA (registration 3043655996) in Wuzhou Guangxi, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 4, 2025. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3043655996
Address
Room 203, Building B1, Xinghua Community, High-tech Industrial Development Zone, Wanxiu District, Wuzhou Guangxi, China, 543000
Owner or operator
Micowey Medical Equipment Guangxi Co., LTD (10095011)
Roles
Manufacturer
First device listed
January 14, 2026
Registered through
2026
Brand names listed
Intense Pulsed Light Therapy Device/MMABM-1

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 4, 2025K251545Intense Pulsed Light Therapy Device (MMABM-1)ONFSubstantially EquivalentMicowey Medical Equipment (Guangxi) Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 4, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.